510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K912244Substantially Equivalent

Urotest Gph

In Wha Pharmaceutical Co., Ltd., Korea, KR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K912244 is the FDA 510(k) clearance record for UROTEST GPH, a class II device, cleared for In Wha Pharmaceutical Co., Ltd. on under FDA product code JII (Atomic Absorption, Lithium). FDA records list one 510(k) clearance for In Wha Pharmaceutical Co., Ltd. As of , FDA records show no recalls naming K912244.

Clearance record

Decision date
Received
(185 days to decision)
Product code
JII Atomic Absorption, Lithium
Regulation
21 CFR 862.3560
Device class
Class II
Review panel
Clinical Toxicology
Applicant
In Wha Pharmaceutical Co., Ltd. Buk-Ku Chungchun-Dong 234-1, Korea, KR
510(k) summary
Statement
Third party review
No

Clearances, product code JII

Trailing 12 months

FDA records hold no clearances under product code JII in the trailing twelve months.

FDA records show no clearances under product code JII in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code JII, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260